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BioMed Research International
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2015
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Article
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Tab 4
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Research Article
Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and Platforms
Table 4
Extra mutations identified using the SureSeq Solid Tumour panel in FFPE gDNA.
Cell line
Gene
Variant
Variant allele frequency
Read depth
639V
TP53
(NM_000546.5)
c.113C>A
5.10%
294
KU-19-19
c.1129A>C
6.64%
271
LUCC3
c.1129A>C
5.10%
255